Overview As a CRA II at ICON, you monitor and support clinical trials to ensure quality, compliance, and patient safety. You will work with investigators and site staff to drive study conduct and data integrity, contributing to study documentation and reports. This home-based role in Barcelona offers meaningful exposure to cutting-edge therapies within a collaborative, values-driven environment. You will leverage your trial experience to advance treatments and new medicines for patients.

Compensaciones / BeneficiosCompetitive base salaryHealth and wellbeing programmesRetirement and pension plansLife assurance and disability coverageEmployee assistance programmes and wellbeing resourcesLearning and development opportunities ResponsabilidadesConduct site qualification, initiation, monitoring, and close-out visits for clinical trialsEnsure protocol compliance, data integrity,



and patient safety throughout the trial processCollaborate with investigators and site staff to facilitate smooth study conductPerform data review and resolution of queries to maintain high-quality clinical dataContribute to preparation and review of study documentation, including protocols and clinical study reports Requisitos principalesBachelor's degree in a scientific or healthcare-related fieldMinimum of 2 years of experience as a Clinical Research AssociateIn-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelinesStrong organizational and communication skills, with attention to detailAbility to work independently and collaboratively in a fast-paced environmentWillingness to travel as required (approximately 60%)Employment with ICON is contingent upon having the legal right to work in the country where the role is based.strong organizational skillsexcellent communicationattention to detailclinical trial processesregulationsICH-GCP guidelines

📌 Clinical Research Associate (Barcelona)
🏢 Jobrapido
📍 Barcelona